An engineered enucleated
mesenchymal stem cell (EMC) and its preparation method and application are disclosed, which can effectively solve the problem of preparing engineered enucleated EMC and realize its application in the preparation of drugs for treating herpesvirus infections. The steps are as follows: Lentiviral
transfection is used to obtain EMC overexpressing
Nectin-1, the overexpression being achieved through
genetic engineering, including
transfection of EMC using a lentiviral vector or adenovirus vector; then, enucleation is performed using discontinuous
density gradient centrifugation to obtain the engineered enucleated EMC. The engineered enucleated EMC of this invention acts as "bait" to competitively capture viruses; the enucleation design fundamentally eliminates the risk of
viral replication and leakage within cells; and the captured viruses are subsequently cleared along with the engineered enucleated EMC's own programmed
apoptosis and subsequent
macrophage phagocytosis, thereby achieving safe and efficient
virus capture and physical clearance.